Proposed Collection; Comment Request; NCI Cancer Genetics Services Directory Web-Based Application Form and Update Mailer, 14034-14035 [2011-6021]
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14034
Federal Register / Vol. 76, No. 50 / Tuesday, March 15, 2011 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; A Generic Submission for
Formative Research, Pretesting,
Stakeholder Measures and Advocate
Forms at NCI
Under the provisions of
Section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, for opportunity
for public comment on proposed data
collection projects, the National Cancer
Institute (NCI), the National Institutes of
Health (NIH) will publish periodic
summaries of proposed projects to be
submitted to the Office of Management
and Budget (OMB) for review and
approval.
Proposed Collection: Title: A Generic
Submission for Formative Research, Pretesting, Stakeholder Measures and
Advocate Forms at NCI. Type of
Information Collection Request: New.
Need and Use of Information Collection:
In order to carry out NCI’s legislative
mandate, the Office of Advocacy
Relations (OAR) disseminates cancer-
SUMMARY:
related information to a variety of
stakeholders, seeks their input and
feedback, and facilitates collaboration
between the Institute and these external
partners to advance NCI’s authorized
programs. It is beneficial for NCI,
through the OAR, to pretest strategies,
concepts, activities and materials while
they are under development.
Additionally, administrative forms may
be part of this generic submission since
they are a necessary part of collecting
demographic information and areas of
interest for advocates. Pre-testing, or
formative evaluation, helps ensure that
the products and services developed by
NCI have the greatest capacity of being
received, understood, and accepted by
their target audiences. Since OAR is
responsible for matching advocates to
NCI programs and initiatives across the
cancer continuum, it is necessary to
measure the satisfaction of both internal
and external stakeholders with this
collaboration. This customer satisfaction
research helps ensure the relevance,
utility, and appropriateness of the many
initiatives and products that OAR and
NCI produce. The OAR will use a
variety of qualitative (focus groups,
interviews) and quantitative (paper,
phone, in-person, and web surveys)
methodologies to conduct this research,
allowing NCI to: (1) Understand
characteristics (attitudes, beliefs, and
behaviors) of the intended target
audience and use this information in the
development of effective strategies,
concepts, activities; (2) use a feedback
loop to help refine, revise, and enhance
OAR’s efforts—ensuring that they have
the greatest relevance, utility,
appropriateness, and impact for/to
target audiences; and (3) expend limited
program resource dollars wisely and
effectively. Frequency of Response: On
occasion. Affected Public: Individuals or
households; Businesses or other for
profit; Not-for-profit institutions and
organizations; Federal Government;
State, Local, or Tribal Government. Type
of Respondents: Adult cancer research
advocates; members of the public;
health care professionals; organizational
representatives. Table 1 outlines the
estimated burden hours required for a
three-year approval of this generic
submission. There are no Capital Costs,
Operating Costs, and/or Maintenance
Costs to report.
TABLE 1—ESTIMATE OF BURDEN HOURS OVER THREE YEARS
[For generic submissions]
Number of
respondents
Survey/Instrument
Frequency of
response
3,600
1,800
225
300
1
1
1
1
Totals ........................................................................................................
srobinson on DSKHWCL6B1PROD with NOTICES
Self-Administered Post-Activity Questionnaires ..............................................
Other Self-Administered Questionnaires and Forms .......................................
Individual In-Depth Interviews .........................................................................
Focus Group Interviews ...................................................................................
5,925
........................
Average time
per response
(minutes/hour)
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies are invited
on one or more of the following points:
(1) Whether the proposed collection of
information is necessary for the proper
performance of the function of the
agency, including whether the
information will have practical utility;
(2) The accuracy of the agency’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) Ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
Ways to minimize the burden of the
collection of information on those who
are to respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
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16:50 Mar 14, 2011
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To
request more information on the
proposed project or to obtain a copy of
the data collection plans, contact
Shannon Bell, Director of Office of
Advocacy Relations (OAR), NCI, NIH,
31 Center Drive, Bldg. 31, Room 10A28,
MSC 2580, Bethesda, MD 20892, call
non-toll-free number 301–451–3393 or
e-mail your request, including your
address to: bells@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60 days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT:
Dated: March 9, 2011.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National
Institutes of Health.
[FR Doc. 2011–6022 Filed 3–14–11; 8:45 am]
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20/60
60/60
60/60
90/60
Annual burden
hours
(.33)
(1.0)
(1.0)
(1.5)
1,200
1,800
225
450
........................
3,675
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; NCI Cancer Genetics
Services Directory Web-Based
Application Form and Update Mailer
Summary: In compliance with the
requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995,
for opportunity for public comment on
proposed data collection projects, the
National Cancer Institute (NCI), the
National Institutes of Health (NIH) will
publish periodic summaries of proposed
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
Proposed Collection: Title: NCI Cancer
Genetics Services Directory Web-based
Application Form and Update Mailer.
E:\FR\FM\15MRN1.SGM
15MRN1
14035
Federal Register / Vol. 76, No. 50 / Tuesday, March 15, 2011 / Notices
Type of Information Collection Request:
Existing Collection in Use Without an
OMB Number. Need and Use of
Information Collection: The purpose of
the online application form and the
Web-based update mailer is to collect
information about genetics professionals
to be included in the NCI Cancer
Genetics Services Directory on NCI’s
Cancer.gov Web site. The information
collected includes name, practice
locations, professional qualifications,
and areas of specialization. Frequency of
Response: Information is collected once
via the online application form, and
then updated annually via the Webbased mailer. Affected Public:
Individuals. Type of Respondents:
Genetics professionals including nurses,
physicians, genetic counselors, and
other professionals who provide
services related to cancer genetics. The
annual reporting burden is estimated at
180 hours (see Table below). There are
no Capital Costs, Operating Costs, and/
or Maintenance Costs to report.
TABLE 1—ESTIMATES OF ANNUAL BURDEN HOURS
Number of
respondents
Tool
Genetics Professionals ...........................
Application Form .........................
60
1
Web-based Update Mailer ..........
600
.....................................................
660
Totals ...............................................
srobinson on DSKHWCL6B1PROD with NOTICES
Average time
per response
minutes/hour
(hours)
Frequency of
response
Type of respondents
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies should
address one or more of the following
points: (1) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the function of the agency, including
whether the information will have
practical utility; (2) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and (4) Minimize the burden
of the collection of information on those
who are to respond, including the use
of appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
For Further Information Contact: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact Margaret Beckwith,
Acting Branch Chief, International
Cancer Research Databank Branch,
Office of Cancer Content Management,
Office of Communication and
Education, National Cancer Institute,
6116 Executive Blvd., Rockville, MD
20852, or call non-toll-free number 301–
496–9096 or e-mail your request,
including your address to:
mbeckwit@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60 days of the date of
this publication.
VerDate Mar<15>2010
16:50 Mar 14, 2011
Jkt 223001
Annual burden
hours
1
30/60
(.50)
15/60
(0.25)
150
........................
........................
180
Dated: March 9, 2011.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National
Institutes of Health.
Dated: March 9, 2011.
Francis S. Collins,
Director, National Institutes of Health.
[FR Doc. 2011–6021 Filed 3–14–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Pursuant to the Federal Advisory
Committee Act, as amended (5 U.S.C.
app.), the Director, National Institutes of
Health (NIH), announces the
establishment of the NCI-Frederick
Advisory Committee.
The Council will provide advice and
recommendations to the Director,
National Cancer Institute (NCI), and the
Associate Director, NCI-Frederick, on
the optimal use of the NCI-Frederick
facility to rapidly meet the most urgent
needs of the NCI. The Committee will
consist of 16 members, including the
Chair, appointed by the Director, NCI.
Members will be authorities
knowledgeable in drug and vaccine
development, clinical trials support,
AIDS research, bioinformatics,
genomics, nanotechnology, biological
repositories, and basic research in
immunology and infectious diseases.
Duration of this committee is
continuing unless formally determined
by the Director, NCI that termination
would be in the best interest of the
public.
Frm 00068
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National Institutes of Health
National Institute of Arthritis and
Musculoskeletal and Skin Diseases;
Notice of Closed Meetings
Notice of Establishment
PO 00000
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Arthritis and Musculoskeletal and Skin
Diseases Special Emphasis Panel; Career
Development, Research Training and
Pathways to Independence Grant Review.
Date: March 29, 2011.
Time: 10 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, One
Democracy Plaza, 6701 Democracy
Boulevard, Bethesda, MD 20892 (Telephone
Conference Call).
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Agencies
[Federal Register Volume 76, Number 50 (Tuesday, March 15, 2011)]
[Notices]
[Pages 14034-14035]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-6021]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment Request; NCI Cancer Genetics
Services Directory Web-Based Application Form and Update Mailer
Summary: In compliance with the requirement of Section
3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity
for public comment on proposed data collection projects, the National
Cancer Institute (NCI), the National Institutes of Health (NIH) will
publish periodic summaries of proposed projects to be submitted to the
Office of Management and Budget (OMB) for review and approval.
Proposed Collection: Title: NCI Cancer Genetics Services Directory
Web-based Application Form and Update Mailer.
[[Page 14035]]
Type of Information Collection Request: Existing Collection in Use
Without an OMB Number. Need and Use of Information Collection: The
purpose of the online application form and the Web-based update mailer
is to collect information about genetics professionals to be included
in the NCI Cancer Genetics Services Directory on NCI's Cancer.gov Web
site. The information collected includes name, practice locations,
professional qualifications, and areas of specialization. Frequency of
Response: Information is collected once via the online application
form, and then updated annually via the Web-based mailer. Affected
Public: Individuals. Type of Respondents: Genetics professionals
including nurses, physicians, genetic counselors, and other
professionals who provide services related to cancer genetics. The
annual reporting burden is estimated at 180 hours (see Table below).
There are no Capital Costs, Operating Costs, and/or Maintenance Costs
to report.
Table 1--Estimates of Annual Burden Hours
----------------------------------------------------------------------------------------------------------------
Average time
Number of Frequency of per response Annual burden
Type of respondents Tool respondents response minutes/hour hours
(hours)
----------------------------------------------------------------------------------------------------------------
Genetics Professionals........ Application Form 60 1 30/60 30
(.50)
Web-based Update 600 1 15/60 150
Mailer. (0.25)
---------------------------------------------------------------------------------
Totals.................... ................ 660 .............. .............. 180
----------------------------------------------------------------------------------------------------------------
Request for Comments: Written comments and/or suggestions from the
public and affected agencies should address one or more of the
following points: (1) Evaluate whether the proposed collection of
information is necessary for the proper performance of the function of
the agency, including whether the information will have practical
utility; (2) Evaluate the accuracy of the agency's estimate of the
burden of the proposed collection of information, including the
validity of the methodology and assumptions used; (3) Enhance the
quality, utility, and clarity of the information to be collected; and
(4) Minimize the burden of the collection of information on those who
are to respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
For Further Information Contact: To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact Margaret Beckwith, Acting Branch Chief,
International Cancer Research Databank Branch, Office of Cancer Content
Management, Office of Communication and Education, National Cancer
Institute, 6116 Executive Blvd., Rockville, MD 20852, or call non-toll-
free number 301-496-9096 or e-mail your request, including your address
to: mbeckwit@mail.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 60 days
of the date of this publication.
Dated: March 9, 2011.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National Institutes of Health.
[FR Doc. 2011-6021 Filed 3-14-11; 8:45 am]
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